Package 71335-2646-2

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 71335-2646-2
Digits Only 7133526462
Product NDC 71335-2646
Product ID 71335-2646_a2cbc9ff-9806-4cdb-9cd4-ec86026f9cf8
Description

30 TABLET in 1 BOTTLE (71335-2646-2)

Marketing

Marketing Status
Marketed Since 2025-06-03
Brand nebivolol
Generic nebivolol
Sample Package No

Linked Drug Pages (1)

Nebivolol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a2cbc9ff-9806-4cdb-9cd4-ec86026f9cf8", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["387013"], "spl_set_id": ["9f0bd0b4-ee17-46bb-b4e2-8ca0ea0e0489"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2646-1)", "package_ndc": "71335-2646-1", "marketing_start_date": "20250603"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2646-2)", "package_ndc": "71335-2646-2", "marketing_start_date": "20250603"}], "brand_name": "Nebivolol", "product_id": "71335-2646_a2cbc9ff-9806-4cdb-9cd4-ec86026f9cf8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2646", "generic_name": "Nebivolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203825", "marketing_category": "ANDA", "marketing_start_date": "20210917", "listing_expiration_date": "20261231"}